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. 2016 Apr 4;3(1):e000147. doi: 10.1136/lupus-2016-000147

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Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

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Relationship between disease activity and size of the CD3⁺CD4⁺CD28⁺CD11a^hiKIR⁺ T cell subset in patients with rheumatic diseases. (A–C) The size of the CD3⁺CD4⁺CD28⁺CD11a^hiKIR⁺ T cell subset in patients is plotted against their disease activity/involvement scores. p Values shown were determined by linear regression. Demographic and disease information for patients and controls analysed is shown in online supplementary table S1. (D) Size of the CD3⁺CD4⁺CD28⁺CD11a^hiKIR⁺ T cell subset from A to C. The numbers in the bars represent the number of subjects studied, and results are presented as the mean±SEM. p Values shown were calculated using Student's t test. Control, healthy subjects, retroperitoneal fibrosis (RPF), systemic lupus erythematosus (SLE) and systemic lupus erythematosus disease activity index (SLEDAI) scores 0–2, 4–5 and ≥6, inactive rheumatoid arthritis (RA(I)), active RA (RA(A)), sine/limited systemic sclerosis (SSc (modified Rodnan skin score (MRSS) 0–2), diffuse systemic sclerosis (SSc (MRSS 9–26)) and Sjögren's syndrome.